Latisha McDaniel

University of Iowa — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

15h-index1.2kcitations22works0.02yr avg
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Research Topics

DNA Repair Mechanisms(4), Eating Disorders and Behaviors(4), Regulation of Appetite and Obesity(4), Genetics and Neurodevelopmental Disorders(4), CRISPR and Genetic Engineering(3)

Publications22 total

Neuronal PAS Domain Proteins 1 and 3 Are Master Regulators of Neuropsychiatric Risk Genes
Biological Psychiatry·2017· 48 citedOpen Access
The Eating-Disorder Associated HDAC4 A778T Mutation Alters Feeding Behaviors in Female Mice
Biological Psychiatry·2016· 20 citedOpen Access
Acute Axonal Degeneration Drives Development of Cognitive, Motor, and Visual Deficits after Blast-Mediated Traumatic Brain Injury in Mice
eNeuro·2016· 67 citedOpen Access
Loss of estrogen-related receptor alpha disrupts ventral-striatal synaptic function in female mice
Neuroscience·2016· 14 citedOpen Access
The Neuropsychiatric Disease-Associated Gene<i>cacna1c</i>Mediates Survival of Young Hippocampal Neurons
eNeuro·2016· 58 citedOpen Access
Erratum: Corrigendum: Wild-type microglia do not reverse pathology in mouse models of Rett syndrome
Nature·2015· 3 citedOpen Access
Wild-type microglia do not reverse pathology in mouse models of Rett syndrome
Nature·2015· 201 citedOpen Access
Behavioral Disturbances in Estrogen-Related Receptor alpha-Null Mice
Cell Reports·2015· 42 citedOpen Access
P7C3 Neuroprotective Chemicals Block Axonal Degeneration and Preserve Function after Traumatic Brain Injury
Cell Reports·2014· 117 citedOpen Access
Double deletion of melanocortin 4 receptors and SAPAP3 corrects compulsive behavior and obesity in mice
Proceedings of the National Academy of Sciences·2013· 42 citedOpen Access
Neuroprotective efficacy of aminopropyl carbazoles in a mouse model of amyotrophic lateral sclerosis
Proceedings of the National Academy of Sciences·2012· 124 citedOpen Access
NCBI Epigenomics: a new public resource for exploring epigenomic data sets
Nucleic Acids Research·2010· 66 citedOpen Access
C008 Array-based comparative genomic hybridization as a clinical assay for genomic profiling in the myelodysplastic syndromes: validation by comparison with conventional cytogenetics and fluorescence in situ hybridization
Leukemia Research·2009· 1 cited
Urinary excretion of acrylamide and metabolites in Fischer 344 rats and B6C3F1 mice administered a single dose of acrylamide
Toxicology Letters·2006· 30 cited
Toxicokinetics of acrylamide and glycidamide in B6C3F mice
Toxicology and Applied Pharmacology·2004· 103 cited
The Gene , Encoding the Human Variant CstF-64 Polyadenylation Protein τCstF-64, Lacks Introns and May Be Associated with Male Sterility
Genomics·2002· 3 cited
THE BLM KNOCKOUT MOUSE
Journal of Neuropathology & Experimental Neurology·1999
PCR-based panel for regional localization of genes on chromosome 15
The American Journal of Human Genetics·1994
Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.
Proceedings of the National Academy of Sciences·1992· 63 citedOpen Access
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
Proceedings of the National Academy of Sciences·1992· 176 citedOpen Access
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Frequent Co-authors

Andrew A. Pieper(10), Jeremiah K. Britt(6), Hector De Jesús‐Cortés(5), Roger A. Schultz(5), Pin Xu(4), Stephanie Tran(4), Whitney Knobbe(4), Paula Huntington(4), Michael Z. Khan(4), Huxing Cui(4), Michael Lutter(4), Ruth Starwalt(3), Terry C. Yin(3), Yuan Lü(3), Jieqi Wang(2), Eike Wegener(2), Teng-Wei Huang(2), Smitha Sripathy(2), Vid Leko(2), Chris S Ward(2)